Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3303376014 | Multiple epiphyseal dysplasia type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3303377017 | Multiple epiphyseal dysplasia type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3303378010 | Polyepiphyseal dysplasia type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401035018 | Multiple epiphyseal dysplasia type 1 (MED 1) is a form of multiple epiphyseal dysplasia that is characterized by normal or mild short stature, pain in the hips and/or knees, progressive deformity of extremities and early-onset osteoarthrosis. Specific features to MED 1 include a more pronounced involvement of hip joints and gait abnormality and a shorter adult height. MED1 is allelic to pseudoachondroplasia with which it shares clinical and radiological features. The disease follows an autosomal dominant mode of transmission. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401036017 | Multiple epiphyseal dysplasia type 1 (MED 1) is a form of multiple epiphyseal dysplasia that is characterised by normal or mild short stature, pain in the hips and/or knees, progressive deformity of extremities and early-onset osteoarthrosis. Specific features to MED 1 include a more pronounced involvement of hip joints and gait abnormality and a shorter adult height. MED1 is allelic to pseudoachondroplasia with which it shares clinical and radiological features. The disease follows an autosomal dominant mode of transmission. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Multiple epiphyseal dysplasia type 1 (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Multiple epiphyseal dysplasia type 1 (disorder) | Is a | Multiple epiphyseal dysplasia | true | Inferred relationship | Some | ||
Multiple epiphyseal dysplasia type 1 (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 3 | |
Multiple epiphyseal dysplasia type 1 (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Multiple epiphyseal dysplasia type 1 (disorder) | Finding site | Bone structure | false | Inferred relationship | Some | 3 | |
Multiple epiphyseal dysplasia type 1 (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 4 | |
Multiple epiphyseal dysplasia type 1 (disorder) | Finding site | Structure of epiphysis | false | Inferred relationship | Some | 4 | |
Multiple epiphyseal dysplasia type 1 (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
Multiple epiphyseal dysplasia type 1 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Multiple epiphyseal dysplasia type 1 (disorder) | Finding site | Structure of epiphysis | true | Inferred relationship | Some | 1 | |
Multiple epiphyseal dysplasia type 1 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Multiple epiphyseal dysplasia type 1 (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Multiple epiphyseal dysplasia type 1 (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 | |
Multiple epiphyseal dysplasia type 1 (disorder) | Interprets | Height / growth measure | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)